New Guinea Impatiens variety SAKIMP051

ABSTRACT

A New Guinea Impatiens plant designated SAKIMP051 is disclosed. Embodiments include seeds of New Guinea Impatiens SAKIMP051, plants of New Guinea Impatiens SAKIMP051, to plant parts of New Guinea Impatiens SAKIMP051, and methods for producing an impatiens plant produced by crossing New Guinea Impatiens SAKIMP051 with itself or with another impatiens variety. Embodiments include methods for producing an impatiens plant containing in its genetic material one or more genes or transgenes and transgenic impatiens plants and plant parts produced by those methods. Embodiments also relate to impatiens varieties, breeding varieties, plant parts, and cells derived from New Guinea Impatiens SAKIMP051, methods for producing other impatiens lines or plant parts derived from New Guinea Impatiens SAKIMP051, and the impatiens plants, varieties, and their parts derived from use of those methods. Embodiments further include hybrid impatiens seeds, plants, and plant parts produced by crossing New Guinea Impatiens SAKIMP051 with another impatiens variety.

BACKGROUND

All publications cited in this application are herein incorporated byreference. New Guinea Impatiens is a species of flowering plants in thefamily Balsaminaeceae.

New Guinea Impatiens can be propagated from seed, cuttings, and tissueculture. Seed, cuttings and tissue culture germination protocols for NewGuinea Impatiens are well-known in the art.

New Guinea Impatiens is an important and valuable ornamental plant.Thus, a continuing goal of ornamental plant breeders is to developplants with novel characteristics, such as color, growth habit, andhardiness. To accomplish this goal, the breeder must select and developplants that have traits that result in superior New Guinea Impatiensvarieties.

The foregoing examples of the related art and limitations relatedtherewith are intended to be illustrative and not exclusive. Otherlimitations of the related art will become apparent to those of skill inthe art upon a reading of the specification.

BRIEF DESCRIPTION OF THE FIGURES

The patent or application file may contain one or more drawings executedin color and/or one or more photographs. Copies of this patent or patentapplication publication with color drawing(s) and/or photograph(s) willbe provided by the Patent Office upon request and payment of thenecessary fee.

FIG. 1 shows the overall plant habit of the plant grown in a pot.

FIG. 2 shows a close-up of a mature flower of the plant.

SUMMARY

The following embodiments and aspects thereof are described inconjunction with systems, tools and methods which are meant to beexemplary, not limiting in scope.

According to one embodiment, there is provided a New Guinea Impatiensplant which is valued as breeding line enabling the development ofsuperior ornamental New Guinea Impatiens plants.

Another embodiment discloses a New Guinea Impatiens plant, wherein asample of representative sample of plant tissue of said New GuineaImpatiens is deposited with a Budapest Depository.

Another embodiment relates to tissue culture produced from protoplastsor cells from the New Guinea Impatiens plants disclosed in the subjectapplication, wherein said cells or protoplasts are produced from a plantpart selected from the group consisting of pollen, ovules, embryos,protoplasts, meristematic cells, callus, leaves, anthers, cotyledons,hypocotyl, pistils, roots, root tips, flowers, seeds, petiole, andstems.

Another embodiment relates to a plant, or a part thereof, produced bygrowing New Guinea Impatiens SAKIMP051, wherein the plant part comprisesat least one cell of New Guinea Impatiens SAKIMP051.

Another embodiment relates to a tissue or cell culture of regenerablecells produced from the plant of SAKIMP051 and a New Guinea Impatiensplant regenerated from the tissue or cell culture of SAKIMP051.

Another embodiment relates to a method of vegetatively propagating theplant of SAKIMP051, comprising the steps of: collecting tissue or cellscapable of being propagated from a plant of SAKIMP051; cultivating saidtissue or cells to obtain proliferated shoots; and rooting saidproliferated shoots to obtain rooted plantlets; or cultivating saidtissue or cells to obtain proliferated shoots, or to obtain plantletsand a plant produced by growing the plantlets or proliferated shoots ofsaid plant.

A further embodiment relates to a method for producing a New GuineaImpatiens seed or embryo, wherein the method comprises crossing aSAKIMP051 plant with a different New Guinea Impatiens plant andharvesting the resultant New Guinea Impatiens seed or embryo.

A further embodiment relates to a method for developing a New GuineaImpatiens plant in a New Guinea Impatiens plant breeding program,comprising applying plant breeding techniques comprising crossing,recurrent selection, mutation breeding, wherein said mutation breedingselects for a mutation that is spontaneous or artificially induced,backcrossing, pedigree breeding, marker enhanced selection,haploid/double haploid production, or transformation to the New GuineaImpatiens plant of SAKIMP051, or its parts, wherein application of saidtechniques results in development of a New Guinea Impatiens plant.

A further embodiment relates to a method of introducing a mutation intothe genome of a New Guinea Impatiens plant SAKIMP051, said methodcomprising mutagenesis of the plant, or plant part thereof, ofSAKIMP051, wherein said mutagenesis is selected from the groupconsisting of temperature, long-term seed storage, tissue cultureconditions, ionizing radiation, chemical mutagens, and targeting inducedlocal lesions in genomes, and wherein the resulting plant comprises atleast one genome mutation and producing plants therefrom.

A further embodiment relates to a method of editing the genome of NewGuinea Impatiens plant SAKIMP051, wherein said method is selected fromthe group comprising zinc finger nucleases, transcription activator-likeeffector nucleases (TALENs), engineered homingendonucleases/meganucleases, and the clustered regularly interspacedshort palindromic repeat (CRISPR)-associated protein9 (Cas9) system, andplants produced therefrom.

A further embodiment relates to a New Guinea Impatiens seed produced bygrowing SAKIMP051.

A further embodiment relates to a method of producing a New GuineaImpatiens plant, or part thereof, by growing a seed produced onSAKIMP051.

In addition to the exemplary aspects and embodiments described above,further aspects and embodiments will become apparent by study of thefollowing descriptions.

DETAILED DESCRIPTION

New Guinea Impatiens variety SAKIMP051 disclosed in the presentapplication has shown uniformity and stability, as described in thefollowing section via vegetative cuttings and tissue culture. New GuineaImpatiens variety SAKIMP051 disclosed in the present application hasbeen asexually reproduced a sufficient number of generations withcareful attention to uniformity of plant type and has been increasedwith continued observation for uniformity. Additionally, New GuineaImpatiens variety SAKIMP051 produces viable pollen and is capable ofbeing used as a parental line in breeding programs.

Origin of SAKIMP051

SAKIMP051 is botanically known as Impatiens×hybrid hort. SAKIMP051originated from an interspecific hybridization in December 2013 betweenfemale ‘NE-533-1’, an unpatented proprietary salmon orange floweredImpatiens breeding line and male ‘NG-424-7H-15H’, an unpatentedproprietary lilac flowered Impatiens breeding line in Misato, Japan.

The F₁ plants were evaluated in Misato, Japan in an open field trial.The criteria for plant selection included deep flower color, compacthabit, and strong root system. At the completion of the trial, onesingle-plant selection was made based on the above criteria andvegetatively propagated. From June to August 2015, the selection wasevaluated in an open field in Misato, Japan. Shoot-tip cuttings of thevariety were then shipped to Salinas, Calif., where the plants wereregenerated and reevaluated for stability of traits. The selectionsubsequently was named ‘SAKIMP051’ and found to have its uniquecharacteristics reproduce true to type in successive generations ofasexual propagation.

Environmental Conditions for Plant Growth

The terminal 1.0 to 1.5 inches of an actively growing stem was excised.The vegetative cuttings were propagated in five to six weeks. The baseof the cuttings were dipped for 1 to 2 seconds in a 1:9 solution of DIP'N GROW (1 solution: 9 water) root inducing solution immediately priorto sticking into the cell trays. Cuttings were stuck into plastic celltrays having 98 cells, and containing a moistened peat moss-basedgrowing medium. The cuttings were misted with water from overhead for 10seconds every 30 minutes until sufficient roots were formed.

Rooted cuttings were transplanted and grown in 6-inch plastic pots in aglass greenhouse located in Salinas, Calif. Pots contained a peatmoss-based growing medium. Soluble fertilizer containing 20% nitrogen,10% phosphorus and 20% potassium was applied once a day or every otherday by overhead irrigation. Plants were fertilized every 2-3 days, 2times in consecutive applications and then given one clear waterapplication. Pots were top-dressed with a dry, slow release fertilizercontaining 14% nitrogen, 14% phosphorus and 14% potassium. The typicalaverage air temperature was 24° C.

Data in Table 1 were taken in Salinas, Calif. Data were obtained fromplants grown about 8 months from propagation by terminal cutting undergreenhouse conditions in Salinas, Calif. Color references are to theRoyal Horticultural Society Colour Chart, 4th edition (2001). Anatomiclabels are from The Cambridge Illustrated Glossary of Botanical Terms,by M. Hickey and C. King, Cambridge University Press.

TABLE 1 VARIETY DESCRIPTION INFORMATION Classification: Family:Balsaminaceae Species: Impatiens intergeneric hybrid (Impatiens ×hybrida hort) Parentage: Female Parent: Proprietary Impatiens plant line‘NE-533-1’ Male Parent: Proprietary Impatiens plant line ‘NG-424-7H-15H’General Appearance, Growth, and Propagation: Habit: Compact Height: 15.0cm to 18.0 cm from soil line to top of foliage Spread: 35.0 cm to 40.0cm Life Cycle: Annual Time to produce a rooted cutting: About 4 weeksTime to bloom from propagation: 6 to 8 weeks Flowering requirements(season): Will flower so long as temperature is above 5° C.Resistance/susceptibility: No particular resistance or susceptibilityobserved Temperature tolerances: Plants observed to continue floweringin a temperature range of 5° C. to 36° C. Stems: Number of branches: 4total with 1 main branch Length of main branch: 2.0 cm from soil line tofirst node Length of secondary branches: 5.0 cm to 6.0 cm from first tosecond node, 16.0 cm to 20.0 cm from first node to end Diameter ofbranches: 1.5 cm to 1.7 cm Diameter of stems off of secondary branches:6.0 mm to 7.0 mm Color of main and secondary branches: RHS N143A (Green)Color of stems off of secondary branches: RHS N144A (Yellow-Green) withRHS 187A (Greyed-Purple) at nodes Anthocyanin color: RHS 187B(Greyed-Purple) Pubescence: Absent Stem description: Strong; circularcross-section, smooth and shiny Internode length: 2.0 cm to 5.0 cmLeaves: Arrangement: Whorled with up to 5 leaves per node, opposite ifonly two leaves at one node Shape: Lanceolate, curled Apex: AcuminateBase: Shortly attenuate Margin: Serrate Surface texture: Dull; waxyLength: 8.7 cm for medium sized leaves Width: 2.5 cm to 3.5 cm onaverage Color: Upper surface: Closest to but darker than RHS 136A(Green) with slight RHS 144A (Yellow-Green) at margins Lower surface:RHS 147B (Yellow-Green) Variegation: Absent Fragrance: Absent Surfacepubescence: Absent Venation: Pinnate Vein color: Upper surface: Closestto RHS 145D (Yellow-Green) Lower surface: RHS 187B (Greyed-Purple)Petiole: Length: 5.0 mm to 1.2 cm Diameter: 2.0 mm to 3.0 mm on mediumsized leaves Color: Closest to RHS 187B with very slight RHS 145B(Yellow-Green) Texture: Smooth, glabrous Flowers: Number of flowers pernode: 1 to 3 in bloom at one time; about 3 to 5 flower buds Number offlowers per plant: Approximately 40 to 50 in bloom Lastingness ofindividual blooms on the plant: 14 days Inflorescence type: Singleflower with spur Fragrance: Absent Corolla: Shape: Roughly circular with5 radial petals Diameter: 4.5 cm Width: 4.5 cm Depth: 4.0 mm Calyx:Sepal Shape: Lanceolate Sepal Number: 2 Sepal Color: Upper surface: Baseof RHS N155B (White) with slight RHS 61A (Red- Purple) and RHS 61B(Red-Purple) with RHS N144C (Yellow-Green) near upper half edge and RHS145C (Yellow-Green) at tip Lower surface: RHS 61A (Red-Purple) with RHS145B (Yellow-Green) at tip Sepal Length: 1.4 cm Sepal diameter: 7.0 mmSepal Base: Subcordate Sepal Apex: Caudate Sepal Margin: Entire Sepaltexture: Glabrous Bud: Surface: Glabrous Length: 1.6 cm Diameter: 1.1 cmShape: Deltoid longitudinal cross-section Color: Closest to but slightlydarker than RHS N74A (Red-Purple) with RHS 187B (Greyed-Purple) at edgePeduncle: Length: 3.9 cm to 4.5 cm Color: Opaque RHS 187C withundertones of RHS 144C Diameter: 2.0 mm Texture: Smooth, glabrousPetals: Pubescence: Glabrous Length: 2.2 cm to 2.8 cm Width: 2.8 to 3.6Shape: Obcordate Apex: Emarginate (cleaved) Margin: Entire Base:Attenuate Petal color: Upper: Closest to but darker and brighter thanRHS N74A (Red-Purple) Lower: Closest to RHS N74A (Red-Purple) Eye zone:Closest to but brighter than RHS 64A (Red-Purple) Spur: Color: RHS 60B(Red-Purple) with hints of RHS N74A (Red-Purple) near base and RHS 145A(Yellow-Green) at tips Shape: Tubular; curved downward Length: 6.7 cmDiameter: 1.0 mm to 2.0 mm Reproductive Organs Stamens: Stamen form:Fused; split into 4 lobes Stamen number: 5 Filament: Free Filamentlength: 4.0 mm Filament color: RHS N144C (Yellow-Green) with slight RHS181D (Greyed-Red) at tip Anther length: 5.0 mm Anther color: Closest toRHS 61A (Red-Purple) Pollen quantity: Abundant Pollen color: RHS 158C(Yellow-White) Pollen description: Powdery Pistil: Pistil number: 1Stigma color: Closest to RHS N199C (Grey-Brown) Style color: RHS 144B(Yellow-Green) with stripe of RHS 187A (Greyed- Purple) Ovaryarrangement: Parietal Ovary interior color: RHS 149A (Yellow-Green) Seedproduction: Not observed

SAKIMP051 is a new and distinct cultivar of New Guinea Impatiens owningto compact growth habit, deep flower color, and strong root system.SAKIMP051 is most similar to the commercial Impatiens varietySUNPATIENS® ‘Compact Neon Pink’ (varietal denomination ‘SAKIMP033’) (USPP26,669); however, there are differences as listed in the table below.

TABLE 2 COMPARISON OF SAKIMP051 WITH ‘SAKIMP033’ CharacteristicSAKIMP051 ‘SAKIMP033’ Growth habit Compact Compact Corolla Diameter 4.5cm 6.5 cm Spur color RHS 60B (Red-Purple) with RHS 145D hints of RHSN74A (Red- (Yellow-Green). Purple) near base and RHS 145A (Yellow-Green)at tips Mature leaf Closest to but darker than RHS 139A color, upper RHS136A (Green) with (Green) surface slight RHS 144A (Yellow- Green) atmargins

SAKIMP051 can be compared with its parental lines, as shown in Table 3:

TABLE 3 COMPARISON OF ‘SAKIMP051 WITH PARENTAL LINES Female Parent MaleParent Characteristic SAKIMP051 ‘NE-533-1’ ‘NG-424-7H-15H’ Flower colorPurple Salmon Orange Lilac Plant Habit Compact More vigorous thanCompact SAKIMP051

Further Embodiments

Breeding with New Guinea Impatiens SAKIMP051

The goal of ornamental plant breeding is to develop new, unique andsuperior ornamental plants. The breeder initially selects and crossestwo or more parental lines, followed by repeated selfing and selection,producing many new genetic combinations. The breeder can theoreticallygenerate billions of different genetic combinations via crossing,selection, selfing and mutations. Therefore, a breeder will neverdevelop the same genetic variety, having the same traits from the exactsame parents.

Each year, the plant breeder selects the germplasm to advance to thenext generation. This germplasm is grown under unique and differentgeographical, climatic and soil conditions and further selections arethen made during and at the end of the growing season. The varietiesthat are developed are unpredictable because the breeder's selectionoccurs in unique environments with no control at the DNA level, and withmillions of different possible genetic combinations being generated. Abreeder of ordinary skill in the art cannot predict the final resultinglines he develops, except possibly in a very gross and general fashion.The same breeder cannot produce the same variety twice by using the sameoriginal parents and the same selection techniques. Thisunpredictability results in the expenditure of large amounts of researchmonies to develop superior impatiens varieties.

Breeding programs combine desirable traits from two or more varieties orvarious broad-based sources into breeding pools from which varieties aredeveloped by selfing and selection of desired phenotypes. Pedigreebreeding is used commonly for the improvement of self-pollinatingplants. Two parents that possess favorable, complementary traits arecrossed to produce an F₁. An F₂ population is produced by selfing one orseveral F_(1s). Selection of the best individuals may begin in the F₂population; then, beginning in the F₃, the best individuals in the bestfamilies are selected. Replicated testing of families can begin in theF₄ generation to improve the effectiveness of selection for traits withlow heritability. At an advanced stage of inbreeding (i.e., F₆ and F₇),the best lines or mixtures of phenotypically similar lines are testedfor potential release as new varieties.

Using New Guinea Impatiens SAKIMP051 to Develop Other Plants

SAKIMP051 plants can also provide a source of breeding material that maybe used to develop new impatiens plants and varieties. Plant breedingtechniques known in the art and used in an impatiens plant breedingprogram include, but are not limited to, recurrent selection, massselection, bulk selection, hybridization, mass selection, backcrossing,pedigree breeding, open-pollination breeding, restriction fragmentlength polymorphism enhanced selection, genetic marker enhancedselection, making double haploids, mutagenesis and transformation. Oftencombinations of these techniques are used. The development of impatiensvarieties in a plant breeding program requires, in general, thedevelopment and evaluation of homozygous varieties. There are manyanalytical methods available to evaluate a new variety. The oldest andmost traditional method of analysis is the observation of phenotypictraits, but genotypic analysis may also be used.

Additional Breeding Methods

Any plants produced using the SAKIMP051 plants disclosed in the presentapplication as at least one parent are also an embodiment. These methodsare well-known in the art and some of the more commonly used breedingmethods are described herein. Descriptions of breeding methods can befound in one of several reference books (e.g., Allard, “Principles ofPlant Breeding” (1999); and Vainstein, “Breeding for Ornamentals:Classical and Molecular Approaches,” Kluwer Academic Publishers (2002);Callaway, “Breeding Ornamental Plants,” Timber Press (2000).

Breeding steps that may be used in the New Guinea Impatiens SAKIMP051plant breeding program can include for example, pedigree breeding,backcrossing, mutation breeding, and recurrent selection. In conjunctionwith these steps, techniques such as RFLP-enhanced selection, geneticmarker enhanced selection (for example, SSR markers), Gene Editing andthe making of double haploids may be utilized.

As used herein, the term “plant” includes plant cells, plantprotoplasts, plant cell tissue cultures from which SAKIMP051 plants canbe regenerated, plant calli, plant clumps, and plant cells that areintact in plants or parts of plants, such as pollen, ovules, embryos,protoplasts, meristematic cells, callus, leaves, anthers, cotyledons,hypocotyl, pistils, roots, root tips, seeds, flowers, petiole, shoot, orstems and the like.

Pedigree Breeding

Pedigree breeding starts with the crossing of two genotypes, such as NewGuinea Impatiens SAKIMP051 and another different impatiens plant havingone or more desirable characteristics that is lacking or whichcomplements the New Guinea Impatiens SAKIMP051 phenotype. If the twooriginal parents do not provide all the desired characteristics, othersources can be included in the breeding population. In the pedigreemethod, superior plants are selfed and selected in successive filialgenerations. In the succeeding filial generations, the heterozygouscondition gives way to homogeneous varieties as a result ofself-pollination and selection. Typically in the pedigree method ofbreeding, five or more successive filial generations of selfing andselection is practiced: F₁ to F₂; F₂ to F₃; F₃ to F₄; F₄ to F₅; etc.After a sufficient amount of inbreeding, successive filial generationswill serve to increase seed of the developed variety. Preferably, thedeveloped variety comprises homozygous alleles at about 95% or more ofits loci.

Backcross Breeding

Backcross breeding has been used to transfer genes for a simplyinherited, highly heritable trait into a desirable homozygous variety orinbred line which is the recurrent parent. The source of the trait to betransferred is called the donor parent. After the initial cross,individuals possessing the phenotype of the donor parent are selectedand repeatedly crossed (backcrossed) to the recurrent parent. Theresulting plant is expected to have the attributes of the recurrentparent and the desirable trait transferred from the donor parent. Thisis also known as single gene conversion and/or backcross conversion.

In addition to being used to create a backcross conversion, backcrossingcan also be used in combination with pedigree breeding. As discussedpreviously, backcrossing can be used to transfer one or morespecifically desirable traits from one variety, the donor parent, to adeveloped variety called the recurrent parent, which has overall goodcommercial characteristics yet lacks that desirable trait or traits.However, the same procedure can be used to move the progeny toward thegenotype of the recurrent parent, but at the same time retain manycomponents of the nonrecurrent parent by stopping the backcrossing at anearly stage and proceeding with selfing and selection. For example, aNew Guinea Impatiens plant may be crossed with another variety toproduce a first generation progeny plant. The first generation progenyplant may then be backcrossed to one of its parent varieties to create aBC₁ or BC₂. Progeny are selfed and selected so that the newly developedvariety has many of the attributes of the recurrent parent and yetseveral of the desired attributes of the nonrecurrent parent. Thisapproach leverages the value and strengths of the recurrent parent foruse in new New Guinea Impatiens varieties.

Therefore, another embodiment is a method of making a backcrossconversion of New Guinea Impatiens SAKIMP051, comprising the steps ofcrossing New Guinea Impatiens SAKIMP051 with a donor plant comprising adesired trait, selecting an F₁ progeny plant comprising the desiredtrait, and backcrossing the selected F₁ progeny plant to New GuineaImpatiens SAKIMP051. This method may further comprise the step ofobtaining a molecular marker profile of New Guinea Impatiens SAKIMP051and using the molecular marker profile to select for a progeny plantwith the desired trait and the molecular marker profile of New GuineaImpatiens SAKIMP051.

Recurrent Selection and Mass Selection

Recurrent selection is a method used in a plant breeding program toimprove a population of plants. New Guinea Impatiens SAKIMP051 issuitable for use in a recurrent selection program. The method entailsindividual plants cross-pollinating with each other to form progeny. Theprogeny are grown and the superior progeny selected by any number ofselection methods, which include individual plant, half-sib progeny,full-sib progeny, and selfed progeny. The selected progeny arecross-pollinated with each other to form progeny for another population.This population is planted and again superior plants are selected tocross-pollinate with each other. Recurrent selection is a cyclicalprocess and therefore can be repeated as many times as desired. Theobjective of recurrent selection is to improve the traits of apopulation. The improved population can then be used as a source ofbreeding material to obtain new varieties for commercial or breedinguse, including the production of a synthetic variety. A syntheticvariety is the resultant progeny formed by the intercrossing of severalselected varieties.

Mass selection is a useful technique when used in conjunction withmolecular marker enhanced selection. In mass selection, seeds fromindividuals are selected based on phenotype or selection requiresgrowing a population of plants in a bulk plot, allowing the plants toself-pollinate, harvesting the seed in bulk, and then using a sample ofthe seed harvested in bulk to plant the next generation. Also, insteadof self-pollination, directed pollination could be used as part of thebreeding program.

Mass and recurrent selections can be used to improve populations ofeither self- or cross-pollinating plants. A genetically variablepopulation of heterozygous individuals is either identified, or created,by intercrossing several different parents. The best plants are selectedbased on individual superiority, outstanding progeny, or excellentcombining ability. The selected plants are intercrossed to produce a newpopulation in which further cycles of selection are continued.

Protoplast Fusion

Also known as somatic fusion, this process can be used with SAKIMP051 tocreate hybrids. The resulting hybrid plants have the chromosomes of eachparent and thus the process is useful for incorporating new traits. Theprotoplast fusion technique is well known in the art; see for exampleHamill J. D., Cocking E. C. (1988) Somatic Hybridization of Plants andits Use in Agriculture. In: Pais M. S. S., Mavituna F., Novais J. M.(eds) Plant Cell Biotechnology. NATO ASI Series (Series H: CellBiology), vol 18.

Mutation Breeding

Mutation breeding is another method of introducing new traits into NewGuinea Impatiens SAKIMP051. Mutations that occur spontaneously or areartificially induced can be useful sources of variability for a plantbreeder. The goal of artificial mutagenesis is to increase the rate ofmutation for a desired characteristic. Mutation rates can be increasedby many different means including temperature, long-term seed storage,tissue culture conditions, ionizing radiation, such as X-rays, Gammarays (e.g., cobalt 60 or cesium 137), neutrons, (product of nuclearfission by uranium 235 in an atomic reactor), Beta radiation (emittedfrom radioisotopes such as phosphorus 32 or carbon 14), or ultravioletradiation (preferably from 2500 to 2900 nm); chemical mutagens (such asbase analogues (5-bromo-uracil)), related compounds (8-ethoxy caffeine),antibiotics (streptonigrin), alkylating agents (sulfur mustards,nitrogen mustards, epoxides, ethylenamines, sulfates, sulfonates such asethyl methanesulfonate, sulfones, lactones), sodium azide,hydroxylamine, nitrous acid, methylnitrilsourea, or acridines; TILLING(targeting induced local lesions in genomes), where mutation is inducedby chemical mutagens and mutagenesis is accompanies by the isolation ofchromosomal DNA from every mutated plant line or seed and screening ofthe population of the seed or plants is performed at the DNA level usingadvanced molecular techniques. Once a desired trait is observed throughmutagenesis the trait may then be incorporated into existing germplasmby traditional breeding techniques. Details of mutation breeding can befound in Vainstein, “Breeding for Ornamentals: Classical and MolecularApproaches,” Kluwer Academic Publishers (2002); Sikora, Per, et al.,“Mutagenesis as a Tool in Plant Genetics, Functional Genomics, andBreeding” International Journal of Plant Genomics. 2011 (2011); 13pages. In addition, mutations created in other New Guinea Impatiensplants may be used to produce a backcross conversion of New GuineaImpatiens that comprises such mutation.

Gene Editing Using CRISPR

Targeted gene editing can be done using CRISPR/Cas9 technology (Saunders& Joung, Nature Biotechnology, 32, 347-355, 2014). CRISPR is a type ofgenome editing system that stands for Clustered Regularly InterspacedShort Palindromic Repeats. This system and CRISPR-associated (Cas) genesenable organisms, such as select bacteria and archaea, to respond to andeliminate invading genetic material. Ishino, Y., et al. J. Bacteriol.169, 5429-5433 (1987). These repeats were known as early as the 1980s inE. coli, but Barrangou and colleagues demonstrated that S. thermophiluscan acquire resistance against a bacteriophage by integrating a fragmentof a genome of an infectious virus into its CRISPR locus. Barrangou, R.,et al. Science 315, 1709-1712 (2007). Many plants have already beenmodified using the CRISPR system. See for example, U.S. ApplicationPublication No. WO2014068346 (György et al., Identification of aXanthomonas euvesicatoria resistance gene from pepper (Capsicum annuum)and method for generating plants with resistance); Martinelli, F. etal., “Proposal of a Genome Editing System for Genetic Resistance toTomato Spotted Wilt Virus” American Journal of Applied Sciences 2014;Noman, A. et al., “CRISPR-Cas9: Tool for Qualitative and QuantitativePlant Genome Editing” Frontiers in Plant Science Vol. 7 November 2016;and “Exploiting the CRISPR/Cas9 System for Targeted Genome Mutagenesisin Petunia” Science Reports Volume 6: February 2016.

Gene editing can also be done using crRNA-guided surveillance systemsfor gene editing. Additional information about crRNA-guided surveillancecomplex systems for gene editing can be found in the followingdocuments, which are incorporated by reference in their entirety: U.S.Application Publication No. 2010/0076057 (Sontheimer et al., Target DNAInterference with crRNA); U.S. Application Publication No. 2014/0179006(Feng, CRISPR-CAS Component Systems, Methods, and Compositions forSequence Manipulation); U.S. Application Publication No. 2014/0294773(Brouns et al., Modified Cascade Ribonucleoproteins and Uses Thereof);Sorek et al., Annu. Rev. Biochem. 82:273-266, 2013; and Wang, S. et al.,Plant Cell Rep (2015) 34: 1473-1476. Therefore, it is another embodimentto use the CRISPR system on New Guinea Impatiens SAKIMP051 to modifytraits and resistances or tolerances to pests, herbicides, diseases, andviruses.

Gene Editing Using TALENs

Transcription activator-like effector nucleases (TALENs) have beensuccessfully used to introduce targeted mutations via repair of doublestranded breaks (DSBs) either through non-homologous end joining (NHEJ),or by homology-directed repair (HDR) and homology-independent repair inthe presence of a donor template. Thus, TALENs are another mechanism fortargeted genome editing using SAKIMP051. The technique is well known inthe art; see for example Malzahn, Aimee et al. “Plant genome editingwith TALEN and CRISPR” Cell & bioscience vol. 7 21. 24 Apr. 2017.

Therefore it is another embodiment to use the TALENs system on NewGuinea Impatiens variety SAKIMP051 to modify traits and resistances ortolerances to pests, herbicides, and viruses.

Other Methods of Genome Editing

In addition to CRISPR and TALENs, two other types of engineerednucleases can be used for genome editing: engineered homingendonucleases/meganucleases (EMNs), and zinc finger nucleases (ZFNs).These methods are well known in the art. See for example, Petilino,Joseph F. “Genome editing in plants via designed zinc finger nucleases”In Vitro Cell Dev Biol Plant. 51(1): pp. 1-8 (2015); and Daboussi,Fayza, et al. “Engineering Meganuclease for Precise Plant GenomeModification” in Advances in New Technology for Targeted Modification ofPlant Genomes. Springer Science+Business. pp 21-38 (2015).

Therefore, it is another embodiment to use engineered nucleases on NewGuinea Impatiens variety SAKIMP051 to modify traits and resistances ortolerances to pests, herbicides, and viruses.

Additional Methods of Transformation

Additional methods include, but are not limited to, expression vectorsintroduced into plant tissues using a direct gene transfer method, suchas microprojectile-mediated delivery, DNA injection, electroporation,and the like. More preferably, expression vectors are introduced intoplant tissues by using either microprojectile-mediated delivery with abiolistic device or by using Agrobacterium-mediated transformation.Transformant plants obtained with the protoplasm of the subject NewGuinea Impatiens SAKIMP051 plants are intended to be within the scope ofthe embodiments of the application.

Single-Gene Conversions

When the term New Guinea Impatiens SAKIMP051 plant is used in thecontext of an embodiment of the present application, this also includesany single gene conversions of New Guinea Impatiens SAKIMP051. The termsingle gene converted plant as used herein refers to those impatiensplants which are developed by a plant breeding technique calledbackcrossing wherein essentially all of the desired morphological andphysiological characteristics of a variety are recovered in addition tothe single gene transferred into the variety via the backcrossingtechnique. Backcrossing methods can be used with one embodiment of thepresent application to improve or introduce a characteristic into thevariety. The term “backcrossing” as used herein refers to the repeatedcrossing of a hybrid progeny back to the recurrent parent, i.e.,backcrossing 1, 2, 3, 4, 5, 6, 7, 8, or more times to the recurrentparent. The parental New Guinea Impatiens plant that contributes thegene for the desired characteristic is termed the nonrecurrent or donorparent. This terminology refers to the fact that the nonrecurrent parentis used one time in the backcross protocol and therefore does not recur.The parental New Guinea Impatiens plant to which the gene or genes fromthe nonrecurrent parent are transferred is known as the recurrent parentas it is used for several rounds in the backcrossing protocol (Poehlman& Sleper (1994). In a typical backcross protocol, the original varietyof interest (recurrent parent) is crossed to a second variety(nonrecurrent parent) that carries the single gene of interest to betransferred. The resulting progeny from this cross are then crossedagain to the recurrent parent and the process is repeated until a NewGuinea Impatiens plant is obtained wherein essentially all of thedesired morphological and physiological characteristics of the recurrentparent are recovered in the converted plant, in addition to the singletransferred gene from the nonrecurrent parent.

The selection of a suitable recurrent parent is an important step for asuccessful backcrossing procedure. The goal of a backcross protocol isto alter or substitute a single trait or characteristic in the originalvariety. To accomplish this, a single gene of the recurrent variety ismodified or substituted with the desired gene from the nonrecurrentparent, while retaining essentially all of the rest of the desiredgenetic, and therefore the desired physiological and morphologicalconstitution of the original variety. The choice of the particularnonrecurrent parent will depend on the purpose of the backcross; one ofthe major purposes is to add some commercially important trait or traitsto the plant. The exact backcrossing protocol will depend on thecharacteristic or trait being altered to determine an appropriatetesting protocol. Although backcrossing methods are simplified when thecharacteristic being transferred is a dominant allele, a recessiveallele may also be transferred. In this instance, it may be necessary tointroduce a test of the progeny to determine if the desiredcharacteristic has been successfully transferred.

Many single gene traits have been identified that are not regularlyselected for in the development of a new variety but that can beimproved by backcrossing techniques. These traits are well-known in theart.

Introduction of a New Trait or Locus into New Guinea Impatiens SAKIMP051

New Guinea Impatiens SAKIMP051 represents a new base of genetics intowhich a new locus or trait may be introgressed. Direct transformationand backcrossing represent two important methods that can be used toaccomplish such an introgression. The term backcross conversion andsingle locus conversion are used interchangeably to designate theproduct of a backcrossing program.

Backcross Conversions of New Guinea Impatiens SAKIMP051

A backcross conversion of New Guinea Impatiens SAKIMP051 occurs when DNAsequences are introduced through backcrossing (Allard, “Principles ofPlant Breeding” (1999) with New Guinea Impatiens SAKIMP051 utilized asthe recurrent parent. Both naturally occurring and transgenic DNAsequences may be introduced through backcrossing techniques. A backcrossconversion may produce a plant with a trait or locus conversion in atleast two or more backcrosses, including at least 2 crosses, at least 3crosses, at least 4 crosses, at least 5 crosses, and the like. Molecularmarker assisted breeding or selection may be utilized to reduce thenumber of backcrosses necessary to achieve the backcross conversion. Forexample, see, Openshaw, S. J., et al., Marker-assisted Selection inBackcross Breeding, Proceedings Symposium of the Analysis of MolecularData, Crop Science Society of America, Corvallis, Oreg. (August 1994),where it is demonstrated that a backcross conversion can be made in asfew as two backcrosses.

The complexity of the backcross conversion method depends on the type oftrait being transferred (single genes or closely linked genes ascompared to unlinked genes), the level of expression of the trait, thetype of inheritance (cytoplasmic or nuclear), and the types of parentsincluded in the cross. It is understood by those of ordinary skill inthe art that for single gene traits that are relatively easy toclassify, the backcross method is effective and relatively easy tomanage. See, Allard, “Principles of Plant Breeding” (1999). Desiredtraits that may be transferred through backcross conversion include, butare not limited to, sterility (nuclear and cytoplasmic), fertilityrestoration, drought tolerance, nitrogen utilization, ornamentalfeatures, disease resistance (bacterial, fungal, or viral), insectresistance, and herbicide resistance. In addition, an introgression siteitself, such as an FRT site, Lox site, or other site specificintegration site, may be inserted by backcrossing and utilized fordirect insertion of one or more genes of interest into a specific plantvariety. In some embodiments, the number of loci that may be backcrossedinto New Guinea Impatiens SAKIMP051 is at least 1, 2, 3, 4, or 5, and/orno more than 6, 5, 4, 3, or 2. A single locus may contain severaltransgenes, such as a transgene for disease resistance that, in the sameexpression vector, also contains a transgene for herbicide resistance.The gene for herbicide resistance may be used as a selectable markerand/or as a phenotypic trait. A single locus conversion of site specificintegration system allows for the integration of multiple genes at theconverted loci.

The backcross conversion may result from either the transfer of adominant allele or a recessive allele. Selection of progeny containingthe trait of interest is accomplished by direct selection for a traitassociated with a dominant allele. Transgenes or genes transferred viabackcrossing typically function as a dominant single gene trait and arerelatively easy to classify. Selection of progeny for a trait that istransferred via a recessive allele requires growing and selfing thefirst backcross generation to determine which plants carry the recessivealleles. Recessive traits may require additional progeny testing insuccessive backcross generations to determine the presence of the locusof interest. The last backcross generation is usually selfed to givepure breeding progeny for the gene(s) being transferred, although abackcross conversion with a stably introgressed trait may also bemaintained by further backcrossing to the recurrent parent withselection for the converted trait.

In addition, the above process and other similar processes describedherein may be used to produce first generation progeny impatiens seed byadding a step at the end of the process that comprises crossing NewGuinea Impatiens SAKIMP051 with the introgressed trait or locus with adifferent plant and harvesting the resultant first generation progenyseed.

Molecular Techniques Using New Guinea Impatiens SAKIMP051

The advent of new molecular biological techniques has allowed theisolation and characterization of genetic elements with specificfunctions. Traditional plant breeding has principally been the source ofnew germplasm, however, advances in molecular technologies have allowedbreeders to provide varieties with novel and much wanted commercialattributes. Molecular techniques such as transformation are popular inbreeding ornamental plants and well-known in the art. See Vainstein,“Breeding for Ornamentals: Classical and Molecular Approaches,” KluwerAcademic Publishers (2002).

Breeding with Molecular Markers

Molecular markers can also be used during the breeding process for theselection of qualitative traits. For example, markers closely linked toalleles or markers containing sequences within the actual alleles ofinterest can be used to select plants that contain the alleles ofinterest during a backcrossing breeding program. The markers can also beused to select for the genome of the recurrent parent and against thegenome of the donor parent. Using this procedure can minimize the amountof genome from the donor parent that remains in the selected plants. Itcan also be used to reduce the number of crosses back to the recurrentparent needed in a backcrossing program. The use of molecular markers inthe selection process is often called genetic marker enhanced selection.Molecular markers may also be used to identify and exclude certainsources of germplasm as parental varieties or ancestors of a plant byproviding a means of tracking genetic profiles through crosses.Molecular markers, which includes markers identified through the use oftechniques such as Isozyme Electrophoresis, Restriction Fragment LengthPolymorphisms (RFLPs), Randomly Amplified Polymorphic DNAs (RAPDs),Arbitrarily Primed Polymerase Chain Reaction (AP-PCR), DNA AmplificationFingerprinting (DAF), Sequence Characterized Amplified Regions (SCARs),Amplified Fragment Length Polymorphisms (AFLPs), Simple Sequence Repeats(SSRs), and Single Nucleotide Polymorphisms (SNPs), may be used in plantbreeding methods utilizing New Guinea Impatiens SAKIMP051. SeeVainstein, “Breeding for Ornamentals: Classical and MolecularApproaches,” Kluwer Academic Publishers (2002).

One use of molecular markers is Quantitative Trait Loci (QTL) mapping.QTL mapping is the use of markers, which are known to be closely linkedto alleles that have measurable effects on a quantitative trait.Selection in the breeding process is based upon the accumulation ofmarkers linked to the positive effecting alleles and/or the eliminationof the markers linked to the negative effecting alleles from the plant'sgenome. See for example, Fletcher, Richard S., et al., “QTL analysis ofroot morphology, flowering time, and yield reveals trade-offs inresponse to drought in Brassica napus” Journal of Experimental Biology.66 (1): 245-256 (2014). QTL markers can also be used during the breedingprocess for the selection of qualitative traits. For example, markersclosely linked to alleles or markers containing sequences within theactual alleles of interest can be used to select plants that contain thealleles of interest during a backcrossing breeding program. The markerscan also be used to select for the genome of the recurrent parent andagainst the genome of the donor parent. Using this procedure canminimize the amount of genome from the donor parent that remains in theselected plants. It can also be used to reduce the number of crossesback to the recurrent parent needed in a backcrossing program. The useof molecular markers in the selection process is often called geneticmarker enhanced selection. Molecular markers may also be used toidentify and exclude certain sources of germplasm as parental varietiesor ancestors of a plant by providing a means of tracking geneticprofiles through crosses.

Production of Double Haploids

The production of double haploids can also be used for the developmentof plants with a homozygous phenotype in the breeding program. Forexample, a New Guinea Impatiens plant for which New Guinea ImpatiensSAKIMP051 is a parent can be used to produce double haploid plants.Double haploids are produced by the doubling of a set of chromosomes(1N) from a heterozygous plant to produce a completely homozygousindividual. This can be advantageous because the process omits thegenerations of selfing needed to obtain a homozygous plant from aheterozygous source. For example, see, Ferrie, Alison M. R., et al.,“Review of Doubled Haploidy Methodologies in Ornamental Species”Propagation of Ornamental Plants. 11(2): pp. 63-77 (2011).

Thus, an embodiment is a process for making a substantially homozygousNew Guinea Impatiens SAKIMP051 progeny plant by producing or obtaining aseed from the cross of New Guinea Impatiens SAKIMP051 and anotherimpatiens plant and applying double haploid methods to the F₁ seed or F₁plant or to any successive filial generation.

In particular, a process of making seed retaining the molecular markerprofile of New Guinea Impatiens SAKIMP051 is contemplated, such processcomprising obtaining or producing F₁ seed for which New Guinea ImpatiensSAKIMP051 is a parent, inducing doubled haploids to create progenywithout the occurrence of meiotic segregation, obtaining the molecularmarker profile of New Guinea Impatiens SAKIMP051, and selecting progenythat retain the molecular marker profile of New Guinea ImpatiensSAKIMP051.

Expression Vectors for New Guinea Impatiens Transformation: Marker Genes

Plant transformation involves the construction of an expression vectorwhich will function in plant cells. Such a vector comprises DNAcomprising a gene under control of, or operatively linked to, aregulatory element (for example, a promoter). Expression vectors includeat least one genetic marker operably linked to a regulatory element (forexample, a promoter) that allows transformed cells containing the markerto be either recovered by negative selection, i.e., inhibiting growth ofcells that do not contain the selectable marker gene, or by positiveselection, i.e., screening for the product encoded by the geneticmarker. Many commonly used selectable marker genes for planttransformation are well-known in the transformation arts, and include,for example, genes that code for enzymes that metabolically detoxify aselective chemical agent which may be an antibiotic or an herbicide, orgenes that encode an altered target which is insensitive to theinhibitor. A few positive selection methods are also known in the art.

One commonly used selectable marker gene for plant transformation is theneomycin phosphotransferase II (nptII) gene which, when under thecontrol of plant regulatory signals, confers resistance to kanamycin.Another commonly used selectable marker gene is the hygromycinphosphotransferase gene which confers resistance to the antibiotichygromycin.

Selectable marker genes for plant transformation not of bacterial origininclude, for example, mouse dihydrofolate reductase, plant5-enolpyruvylshikimate-3-phosphate synthase, and plant acetolactatesynthase (Eichholtz, et al., Somatic Cell Mol. Genet., 13:67 (1987);Shah, et al., Science, 233:478 (1986); Charest, et al., Plant Cell Rep.,8:643 (1990)).

Another class of marker genes for plant transformation requiresscreening of presumptively transformed plant cells, rather than directgenetic selection of transformed cells, for resistance to a toxicsubstance such as an antibiotic. These genes are particularly useful toquantify or visualize the spatial pattern of expression of a gene inspecific tissues and are frequently referred to as reporter genesbecause they can be fused to a gene or gene regulatory sequence for theinvestigation of gene expression. Commonly used marker genes forscreening presumptively transformed cells include β-glucuronidase (GUS),β-galactosidase, luciferase, and chloramphenicol acetyltransferase(Jefferson, R. A., Plant Mol. Biol. Rep., 5:387 (1987); Teeri, et al.,EMBO J., 8:343 (1989); Koncz, et al., Proc. Natl. Acad. Sci. USA, 84:131(1987); DeBlock, et al., EMBO J., 3:1681 (1984)).

Expression Vectors for New Guinea Impatiens Transformation: Promoters

Genes included in expression vectors must be driven by a nucleotidesequence comprising a regulatory element (for example, a promoter).Several types of promoters are well known in the transformation arts asare other regulatory elements that can be used alone or in combinationwith promoters.

As used herein, “promoter” includes reference to a region of DNAupstream from the start of transcription and involved in recognition andbinding of RNA polymerase and other proteins to initiate transcription.A “plant promoter” is a promoter capable of initiating transcription inplant cells. Examples of promoters under developmental control includepromoters that preferentially initiate transcription in certain tissues,such as leaves, roots, seeds, fibers, xylem vessels, tracheids, orsclerenchyma. Such promoters are referred to as “tissue-preferred.”Promoters that initiate transcription only in a certain tissue arereferred to as “tissue-specific.” A “cell-type” specific promoterprimarily drives expression in certain cell types in one or more organs,for example, vascular cells in roots or leaves. An “inducible” promoteris a promoter which is under environmental control. Examples ofenvironmental conditions that may affect transcription by induciblepromoters include anaerobic conditions or the presence of light.Tissue-specific, tissue-preferred, cell-type specific, and induciblepromoters constitute the class of “non-constitutive” promoters. A“constitutive” promoter is a promoter that is active under mostenvironmental conditions. Many types of promoters are well known in theart.

Signal Sequences for Targeting Proteins to Subcellular Compartments

Transport of a protein produced by transgenes to a subcellularcompartment, such as the chloroplast, vacuole, peroxisome, glyoxysome,cell wall, or mitochondrion, or for secretion into the apoplast, isaccomplished by means of operably linking the nucleotide sequenceencoding a signal sequence to the 5′ and/or 3′ region of a gene encodingthe protein of interest. Targeting sequences at the 5′ and/or 3′ end ofthe structural gene may determine during protein synthesis andprocessing where the encoded protein is ultimately compartmentalized.Many signal sequences are well-known in the art. See, for example,Becker, et al., Plant Mol. Biol., 20:49 (1992); Knox, C., et al., PlantMol. Biol., 9:3-17 (1987); Lerner, et al., Plant Physiol., 91:124-129(1989); Frontes, et al., Plant Cell, 3:483-496 (1991); Matsuoka, et al.,Proc. Natl. Acad. Sci., 88:834 (1991); Gould, et al., J Cell. Biol.,108:1657 (1989); Creissen, et al., Plant 1, 2:129 (1991); Kalderon, etal., Cell, 39:499-509 (1984); Steifel, et al., Plant Cell, 2:785-793(1990).

Foreign Protein Genes: Transformation

Various promoters, targeting sequences, enhancing sequences, and otherDNA sequences can be inserted into the genome for the purpose ofaltering the expression of genes

Gene Silencing and Altering Gene Expression

Many techniques for altering gene expression are well-known to one ofskill in the art, including, but not limited to, knock-outs (such as byinsertion of a transposable element such as Mu (Vicki Chandler, TheMaize Handbook, Ch. 118 (Springer-Verlag 1994)) or other geneticelements such as a FRT, Lox, or other site specific integration sites;antisense technology (see, e.g., Sheehy, et al., PNAS USA, 85:8805-8809(1988) and U.S. Pat. Nos. 5,107,065, 5,453,566, and 5,759,829);co-suppression (e.g., Taylor, Plant Cell, 9:1245 (1997); Jorgensen,Trends Biotech., 8(12):340-344 (1990); Flavell, PNAS USA, 91:3490-3496(1994); Finnegan, et al., Bio/Technology, 12:883-888 (1994); Neuhuber,et al., Mol. Gen. Genet., 244:230-241 (1994)); RNA interference (Napoli,et al., Plant Cell, 2:279-289 (1990); U.S. Pat. No. 5,034,323; Sharp,Genes Dev., 13:139-141 (1999); Zamore, et al., Cell, 101:25-33 (2000);Montgomery, et al., PNAS USA, 95:15502-15507 (1998)), virus-induced genesilencing (Burton, et al., Plant Cell, 12:691-705 (2000); Baulcombe,Curr. Op. Plant Bio., 2:109-113 (1999)); target-RNA-specific ribozymes(Haseloff, et al., Nature, 334:585-591 (1988)); hairpin structures(Smith, et al., Nature, 407:319-320 (2000); U.S. Pat. Nos. 6,423,885,7,138,565, 6,753,139, and 7,713,715); MicroRNA (Aukerman & Sakai, PlantCell, 15:2730-2741 (2003)); ribozymes (Steinecke, et al., EMBO J.,11:1525 (1992); Perriman, et al., Antisense Res. Dev., 3:253 (1993));oligonucleotide mediated targeted modification (e.g., U.S. Pat. Nos.6,528,700 and 6,911,575); Zn-finger targeted molecules (e.g., U.S. Pat.Nos. 7,151,201, 6,453,242, 6,785,613, 7,177,766 and 7,788,044);transposable elements (e.g. Dubin, M. J., et al., Transposons: ablessing curse, Current opinion in plant biology, Vol: 42, Page: 23-29,2018 and Eric T. Johnson, Jesse B. Owens & Stefan Moisyadi (2016) Vastpotential for using the piggyBac transposon to engineer transgenicplants at specific genomic locations, Bioengineered, 7:1, 3-6); andother methods or combinations of the above methods known to those ofskill in the art.

Additional Transformation Embodiments

The foregoing methods for transformation may be used for producing atransgenic variety. The transgenic variety could then be crossed withanother (non-transformed or transformed) variety in order to produce anew transgenic variety. Alternatively, a genetic trait that has beenengineered into a particular New Guinea Impatiens line using theforegoing transformation techniques could be moved into another lineusing traditional backcrossing techniques that are well known in theplant breeding arts. For example, a backcrossing approach could be usedto move an engineered trait from a public, non-elite variety into anelite variety, or from a variety containing a foreign gene in its genomeinto a variety or varieties that do not contain that gene. As usedherein, “crossing” can refer to a simple x by y cross or the process ofbackcrossing depending on the context.

Likewise, by means of one embodiment, commercially important genes canbe expressed in transformed plants. More particularly, plants can begenetically engineered to express various phenotypes of commercialinterest, including, but not limited to, genes that confer resistance topests or disease, genes that confer resistance to an herbicide, genesthat confer or contribute to a value-added or desired trait, genes thatcontrol male sterility, genes that create a site for site specific DNAintegration, and genes that affect abiotic stress resistance. Manyhundreds if not thousands of different genes are known and couldpotentially be introduced into a New Guinea Impatiens plant according tothe invention. Non-limiting examples of particular genes andcorresponding phenotypes one may choose to introduce into a New GuineaImpatiens plant include one or more genes for insect tolerance, such asa Bacillus thuringiensis (B_(t).) gene, pest tolerance such as genes forfungal disease control, herbicide tolerance such as genes conferringglyphosate tolerance, and genes for quality improvements such asenvironmental or stress tolerances, or any desirable changes in plantphysiology, growth, development, morphology or plant product(s). Forexample, structural genes would include any gene that confers insecttolerance including but not limited to a Bacillus insect control proteingene as described in WO 99/31248, herein incorporated by reference inits entirety, U.S. Pat. No. 5,689,052, herein incorporated by referencein its entirety, U.S. Pat. Nos. 5,500,365 and 5,880,275, hereinincorporated by reference in their entirety. In another embodiment, thestructural gene can confer tolerance to the herbicide glyphosate asconferred by genes including, but not limited to Agrobacterium strainCP4 glyphosate resistant EPSPS gene (aroA:CP4) as described in U.S. Pat.No. 5,633,435, herein incorporated by reference in its entirety, orglyphosate oxidoreductase gene (GOX) as described in U.S. Pat. No.5,463,175, herein incorporated by reference in its entirety.Alternatively, the DNA coding sequences can affect these phenotypes byencoding a non-translatable RNA molecule that causes the targetedinhibition of expression of an endogenous gene, for example viaantisense- or cosuppression-mediated mechanisms (see, for example, Birdet al., Biotech. Gen. Engin. Rev., 9:207, 1991). The RNA could also be acatalytic RNA molecule (i.e., a ribozyme) engineered to cleave a desiredendogenous mRNA product (see for example, Gibson and Shillito, Mol.Biotech., 7:125, 1997). Thus, any gene which produces a protein or mRNAwhich expresses a phenotype or morphology change of interest is usefulfor the practice of one or more embodiments.

Tissue Culture

Further reproduction of the variety can occur by tissue culture andregeneration. Tissue culture of various tissues of ornamental plants andNew Guinea Impatiens SAKIMP051 and regeneration of plants therefrom iswell-known and widely published. For example, reference may be had to doValla Rego, Luciana et al., Crop Breeding and Applied Technology. 1(3):283-300 (2001); Komatsuda, T., et al., Crop Sci., 31:333-337 (1991);Stephens, P. A., et al., Theor. Appl. Genet., 82:633-635 (1991);Komatsuda, T., et al., Plant Cell, Tissue and Organ Culture, 28:103-113(1992); Dhir, S., et al., Plant Cell Reports, 11:285-289 (1992); Pandey,P., et al., Japan J. Breed., 42:1-5 (1992); and Shetty, K., et al.,Plant Science, 81:245-251 (1992). Thus, another embodiment is to providecells which upon growth and differentiation produce New Guinea Impatiensplants having the physiological and morphological characteristics of NewGuinea Impatiens SAKIMP051 described in the present application.

Regeneration refers to the development of a plant from tissue culture.The term “tissue culture” indicates a composition comprising isolatedcells of the same or a different type or a collection of such cellsorganized into parts of a plant. Exemplary types of tissue cultures areprotoplasts, calli, plant clumps, and plant cells that can generatetissue culture that are intact in plants or parts of plants, such aspollen, ovules, embryos, protoplasts, meristematic cells, callus,pollen, leaves, ovules, anthers, cotyledons, hypocotyl, pistils, roots,root tips, flowers, seeds, petiole, shoot, or stems, and the like. Meansfor preparing and maintaining plant tissue culture are well-known in theart.

While a number of exemplary aspects and embodiments have been discussedabove, those of skill in the art will recognize certain modifications,permutations, additions and sub-combinations thereof. It is thereforeintended that the following appended claims and claims hereafterintroduced are interpreted to include all such modifications,permutations, additions, and sub-combinations as are within their truespirit and scope.

One or more aspects may be embodied in other specific forms withoutdeparting from its spirit or essential characteristics. The describedembodiments are to be considered in all respects only as illustrativeand not restrictive. The scope of the embodiments is, therefore,indicated by the appended claims rather than by the foregoingdescription. All changes which come within the meaning and range ofequivalency of the claims are to be embraced within their scope. Theforegoing discussion of the embodiments has been presented for purposesof illustration and description. The foregoing is not intended to limitthe embodiments to the form or forms disclosed herein. In the foregoingDetailed Description for example, various features of the embodimentsare grouped together in one or more embodiments for the purpose ofstreamlining the disclosure. This method of disclosure is not to beinterpreted as reflecting an intention that the claimed embodimentsrequire more features than are expressly recited in each claim. Rather,as the following claims reflect, inventive aspects lie in less than allfeatures of a single foregoing disclosed embodiment. Thus, the followingclaims are hereby incorporated into this Detailed Description, with eachclaim standing on its own as a separate preferred embodiment.

Moreover, though the description of the embodiments has includeddescription of one or more embodiments and certain variations andmodifications, other variations and modifications are within the scopeof the embodiments (e.g., as may be within the skill and knowledge ofthose in the art, after understanding the present disclosure). It isintended to obtain rights which include alternative embodiments to theextent permitted, including alternate, interchangeable and/or equivalentstructures, functions, ranges or acts to those claimed, whether or notsuch alternate, interchangeable and/or equivalent structures, functions,ranges or acts are disclosed herein, and without intending to publiclydedicate any patentable subject matter.

The use of the terms “a,” “an,” and “the,” and similar referents in thecontext of describing the embodiments (especially in the context of thefollowing claims) are to be construed to cover both the singular and theplural, unless otherwise indicated herein or clearly contradicted bycontext. The terms “comprising,” “having,” “including,” and “containing”are to be construed as open-ended terms (i.e., meaning “including, butnot limited to,”) unless otherwise noted. Recitation of ranges of valuesherein are merely intended to serve as a shorthand method of referringindividually to each separate value falling within the range, unlessotherwise indicated herein, and each separate value is incorporated intothe specification as if it were individually recited herein. Forexample, if the range 10-15 is disclosed, then 11, 12, 13, and 14 arealso disclosed. All methods described herein can be performed in anysuitable order unless otherwise indicated herein or otherwise clearlycontradicted by context. The use of any and all examples, or exemplarylanguage (e.g., “such as”) provided herein, is intended merely to betterilluminate the embodiments and does not pose a limitation on the scopeof the embodiments unless otherwise claimed. No language in thespecification should be construed as indicating any non-claimed elementas essential to the practice one or more embodiments.

DEPOSIT INFORMATION

A deposit of the Sakata Seed Corporation proprietary New GuineaImpatiens variety SAKIMP051 plant tissue disclosed above and recited inthe appended claims has been made with the Provasoli-Guillard NationalCenter for Marine Algae and Microbiota, Bigelow Laboratory for OceanSciences (NCMA), 60 Bigelow Drive, East Boothbay, Me 04544. The date ofdeposit was Apr. 1, 2020. The NCMA No. is 202004001. The deposit ofplant tissue was taken from the same deposit maintained by Sakata SeedCorporation since prior to the filing date of this application. Thedeposit will be maintained in the NCMA depository for a period of 30years, or 5 years after the most recent request, or for the enforceablelife of the patent, whichever is longer, and will be replaced ifnecessary, during that period. Upon issuance, all restrictions on theavailability to the public of the deposit will be irrevocably removedconsistent with all of the requirements of 37 C.F.R. §§ 1.801-1.809.

What is claimed is:
 1. A plant of New Guinea Impatiens varietySAKIMP051, wherein a representative sample of plant tissue of saidcultivar was deposited under NCMA No.
 202004001. 2. A plant, or a plantpart thereof produced by growing the plant of claim 1, wherein the plantor plant part comprises at least one cell of New Guinea Impatiensvariety SAKIMP051.
 3. A New Guinea Impatiens plant, or part thereof,having all of the physiological and morphological characteristics of theNew Guinea Impatiens plant of claim
 1. 4. A tissue or cell culture ofregenerable cells produced from the plant of claim
 1. 5. The tissue orcell culture of claim 4, comprising tissues or cells from a plant partselected from the group consisting of leaves, pollen, embryos,cotyledons, hypocotyl, meristematic cells, roots, root tips, pistils,anthers, flowers, and stems.
 6. A New Guinea Impatiens plant regeneratedfrom the tissue or cell culture of claim 5, wherein said plant has allof the morphological and physiological characteristics of New GuineaImpatiens SAKIMP051 listed in Table
 1. 7. A method of vegetativelypropagating the plant of claim 1, comprising the steps of: collectingtissue or cells capable of being propagated from said plant; cultivatingsaid tissue or cells to obtain proliferated shoots; and rooting saidproliferated shoots to obtain rooted plantlets; or cultivating saidtissue or cells to obtain proliferated shoots, or to obtain plantlets.8. A New Guinea Impatiens plant produced by growing the plantlets orproliferated shoots of claim
 7. 9. A method for producing an embryo orseed, wherein the method comprises crossing the plant of claim 1 withanother plant and harvesting the resultant embryo or seed.
 10. A methodof determining the genotype of the New Guinea Impatiens plant of claim1, wherein said method comprises obtaining a sample of nucleic acidsfrom said plant and detecting in said nucleic acids a plurality ofpolymorphisms.
 11. A method of producing a New Guinea Impatiens plantresistant to the group consisting of herbicides, insecticides, anddisease, wherein the method comprises transforming the New GuineaImpatiens plant of claim 1 with a transgene, and wherein said transgeneconfers resistance to an herbicide, insecticide, or disease.
 12. Anherbicide, insecticide, or disease resistant plant produced by themethod of claim
 11. 13. A method for developing a New Guinea Impatiensplant in a plant breeding program, comprising applying plant breedingtechniques comprising crossing, recurrent selection, mutation breeding,wherein said mutation breeding selects for a mutation that isspontaneously or naturally induced or artificially induced,backcrossing, pedigree breeding, marker enhanced selection,haploid/double haploid production, or transformation to the New GuineaImpatiens plant of claim 1, or its parts, wherein application of saidtechniques results in development of a New Guinea Impatiens plant.
 14. Amethod of introducing a mutation into the genome of New Guinea Impatiensplant SAKIMP051, said method comprising mutagenesis of the plant, orplant part thereof, of claim 1, wherein said mutagenesis is selectedfrom the group consisting of temperature, long-term seed storage, tissueculture conditions, ionizing radiation, chemical mutagens, or targetinginduced local lesions in genomes, and wherein the resulting plantcomprises at least one genome mutation.
 15. A method of editing thegenome of New Guinea Impatiens plant, or a plant part of, SAKIMP051,wherein a representative sample of plant tissue of said cultivar wasdeposited under NCMA No. 202004001, wherein said method is selected fromthe group comprising zinc finger nucleases, transcription activator-likeeffector nucleases (TALENs), engineered homingendonucleases/meganucleases, and the clustered regularly interspacedshort palindromic repeat (CRISPR)-associated protein9 (Cas9) system. 16.A New Guinea Impatiens plant produced by the method of claim
 15. 17. ANew Guinea Impatiens seed produced by growing the plant of claim
 1. 18.A method of producing a New Guinea Impatiens plant, or part thereof,produced by growing the seed of claim
 17. 19. A seed or embryo producedby the method of claim wherein the female parent is SAKIMP051.
 20. Themethod of claim 9, further comprising producing a plant, or a partthereof, from the resultant embryo or seed.